From screen to target: insights and approaches for the development of anti-virulence compounds

被引:16
作者
Beckham, Katherine S. H. [1 ]
Roe, Andrew J. [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Glasgow Biomed Res Ctr, Inst Infect Immun & Inflammat, Glasgow G12 8TA, Lanark, Scotland
关键词
infection; anti-virulence; secretion; inhibitor; Escherichia coli; ENTERICA SEROVAR TYPHIMURIUM; SECRETION SYSTEM INHIBITORS; SMALL-MOLECULE INHIBITORS; III PROTEIN SECRETION; SALICYLIDENE ACYLHYDRAZIDE; CHLAMYDIA-TRACHOMATIS; IDENTIFICATION; PATHOGENS; YERSINIA; CYCLE;
D O I
10.3389/fcimb.2014.00139
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A detailed understanding of host-pathogen interactions provides exciting opportunities to interfere with the infection process. Anti-virulence compounds aim to modulate or pacify pathogenesis by reducing expression of critical virulence determinants. In particular, prevention of attachment by inhibiting adhesion mechanisms has been the subject of intense research. Whilst it has proven relatively straightforward to develop robust screens for potential anti-virulence compounds, understanding their precise mode of action has proven much more challenging. In this review we illustrate this challenge from our own experiences working with the salicylidene acylhydrazide group of compounds. We aim to provide a useful perspective to guide researchers interested in this field and to avoid some of the obvious pitfalls.
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页数:8
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